About us Chiesi is an international research-focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a
Providing hands‑on scientific and technical leadership in process insourcing, technology transfer, scale‑up, and validation activities Coordinating upstream process development, optimization, and industrialization activities with internal R&D teams and external CMOs Leading lifecycle management activities for commercial
Principal Regulatory Writer, Global Rare Diseases Department: GRD Regulatory Affairs Business Area: R&D, Pharmacovigilance & Regulatory Affairs Job Type: Direct Employee Contract Type: Permanent Location: Parma, IT What we are looking for This is what you
CHIESI is an international research‑focused biopharmaceutical group with 90 years’ experience, operating in more than 30 countries, with its Headquarter in Parma, Italy. More than 8,000 employees across the group are united by a singular purpose:
- Providing hands‑on scientific and technical leadership in process insourcing, technology transfer, scale‑up, and validation activities - Coordinating upstream process development, optimization, and industrialization activities with internal R&D teams and external CMOs - Leading lifecycle management
Experteer Overview As a senior leader in Global TechOp&S, you will drive the industrialization and lifecycle management of upstream biopharmaceutical processes. You will lead insourcing, technology transfer, scale‑up and validation to ensure robust, scalable manufacturing from
